Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008753-04
Application #
6628728
Study Section
Special Emphasis Panel (ZGM1-BRT-5 (01))
Program Officer
Rhoades, Marcus M
Project Start
2000-07-01
Project End
2005-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
4
Fiscal Year
2003
Total Cost
$250,640
Indirect Cost
Name
Yale University
Department
Genetics
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Li, Peining; Pomianowski, Pawel; DiMaio, Miriam S et al. (2011) Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization. Am J Med Genet A 155A:1605-15
Martinez, Ivan; Cazalla, Demian; Almstead, Laura L et al. (2011) miR-29 and miR-30 regulate B-Myb expression during cellular senescence. Proc Natl Acad Sci U S A 108:522-7
Rossi, Michael R; DiMaio, Miriam S; Xiang, Bixia et al. (2009) Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature. Am J Med Genet A 149A:2788-94
Klein, Roger D; Thorland, Erik C; Gonzales, Patrick R et al. (2006) A multiplex assay for the detection and mapping of complex glycerol kinase deficiency. Clin Chem 52:1864-70
Zhang, Hui Z; Degar, Barbara A; Rogoulina, Svetlana et al. (2006) Hematopoiesis following disruption of the Pitx2 homeodomain gene. Exp Hematol 34:167-78
Li, Peining; Zhang, Hui Z; Huff, Shannon et al. (2006) Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement. Am J Med Genet A 140:2721-9
Busygina, Valeria; Kottemann, Molly C; Scott, Kenneth L et al. (2006) Multiple endocrine neoplasia type 1 interacts with forkhead transcription factor CHES1 in DNA damage response. Cancer Res 66:8397-403
Klein, Roger D; Salih, Sana; Bessoni, Jesse et al. (2005) Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory. Genet Med 7:131-8
Klein, Roger D; Dykas, Daniel J; Bale, Allen E (2005) Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory. Genet Med 7:611-9
Zhang, Hui Z; Li, Peining; Wang, Dongmei et al. (2004) FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6. Am J Med Genet A 124A:280-7

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